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The Effects of Two Functional Electrical Stimulation Cycling Paradigms

Primary Purpose

Spinal Cord Injury

Status
Completed
Phase
Phase 2
Locations
United States
Study Type
Interventional
Intervention
Cycling with functional electrical stimulation
Sponsored by
Thomas Jefferson University
About
Eligibility
Locations
Arms
Outcomes
Full info

About this trial

This is an interventional treatment trial for Spinal Cord Injury focused on measuring Spinal Cord Injury, Cycling, Functional Electrical Stimulation

Eligibility Criteria

18 Years - 65 Years (Adult, Older Adult)All SexesDoes not accept healthy volunteers

Inclusion Criteria:

  • Cervical or thoracic SCI of greater than 6 months duration
  • American Spinal Injury Association Impairment Scale (AIS) levels A (motor and sensory complete) or B (motor complete)
  • Intact lower motor neurons to the quadriceps, hamstrings, and gluteal muscles

Exclusion Criteria:

  • History of renal or bladder stones or renal impairment
  • Presence of conditions that require chronic steroids
  • Symptomatic or known cardiac disease
  • Pulmonary disease limiting exercise tolerance
  • Ventilator dependency
  • Implanted devices that may be adversely affected by the FES system
  • Lower extremity fragility fractures in the previous 3 months
  • Severe spasticity in legs
  • Presence of a Grade 2 or higher pressure ulcer
  • Severely limited range of joint motion
  • Heterotopic ossification of joints in the lower extremities
  • Uncontrolled autonomic dysreflexia
  • Dislocation of one or both hips
  • Pregnancy or plans to become pregnant during the study
  • Post menopausal, if female
  • Current seizure disorder
  • Participation in activities involving electrical stimulation or activity based therapy within the past 3 months
  • Participation in a neuroregenerative intervention within the past 12 months

Sites / Locations

  • Magee Rehabilitation Hospital
  • Thomas Jefferson University Hospital
  • Thomas Jefferson University

Arms of the Study

Arm 1

Arm 2

Arm Type

Experimental

Experimental

Arm Label

High cadence, low resistance

Low cadence, high resistance

Arm Description

Subjects in this arm will cycle with functional electrical stimulation at a higher cadence (speed) and a lower resistance.

Subjects in this arm will cycle with functional electrical stimulation at a lower cadence (speed) and a higher resistance.

Outcomes

Primary Outcome Measures

Bone density and bone microarchitecture
Bone is measured using dexascan and Magnetic Resonance Imaging (MRI) to examine different types of bone (cortical and trabecular).
Bone density and bone microarchitecture
Bone is measured using dexascan and Magnetic Resonance Imaging (MRI) to examine different types of bone (cortical and trabecular).
Muscle volume
Muscle volume is assessed using MRI
Muscle volume
Muscle volume is assessed using MRI

Secondary Outcome Measures

Muscle strength
Muscle strength is assessed by stimulating the muscle using a max twitch technique and measuring the isometric force output on a dynamometer.
Muscle strength
Muscle strength is assessed by stimulating the muscle using a max twitch technique and measuring the isometric force output on a dynamometer.
Muscle strength
Muscle strength is assessed by stimulating the muscle using a max twitch technique and measuring the isometric force output on a dynamometer.
Bone markers
Bone markers are assessed through blood and urine analysis.
Bone markers
Bone markers are assessed through blood and urine analysis.
Bone markers
Bone markers are assessed through blood and urine analysis.
Fat free soft tissue
Fat free mass is assessed using a bioimpedance monitor.
Fat free soft tissue
Fat free mass is assessed using a bioimpedance monitor.
Fat free soft tissue
Fat free mass is assessed using a bioimpedance monitor.

Full Information

First Posted
November 15, 2010
Last Updated
January 7, 2014
Sponsor
Thomas Jefferson University
Collaborators
The Craig H. Neilsen Foundation, Magee Rehabilitation Hospital, Temple University, University of Delaware
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1. Study Identification

Unique Protocol Identification Number
NCT01244594
Brief Title
The Effects of Two Functional Electrical Stimulation Cycling Paradigms
Official Title
The Effects of Two Functional Electrical Stimulation Cycling Paradigms
Study Type
Interventional

2. Study Status

Record Verification Date
January 2014
Overall Recruitment Status
Completed
Study Start Date
July 2010 (undefined)
Primary Completion Date
October 2013 (Actual)
Study Completion Date
October 2013 (Actual)

3. Sponsor/Collaborators

Responsible Party, by Official Title
Sponsor
Name of the Sponsor
Thomas Jefferson University
Collaborators
The Craig H. Neilsen Foundation, Magee Rehabilitation Hospital, Temple University, University of Delaware

4. Oversight

Data Monitoring Committee
No

5. Study Description

Brief Summary
Background: People with spinal cord injury (SCI) are at risk for many health conditions, some of which can be decreased with exercise. Cycling with Functional Electrical Stimulation (FES) is one way to obtain exercise after SCI. However, cycling with FES has only been done one way, which involves pedaling more quickly with less force to work against. Pedaling more slowly would allow the person to work against more force, which may lead to greater improvements in bone mineral density and muscle size. It may also lead to greater changes in bone make-up, body fat, and cholesterol levels. All of these improvements may lead to a decrease in bone fractures and cardiovascular disease, two major medical issues that exist in the SCI population. Study Aims: This study will compare the outcomes on bone, muscle and cardiovascular health between the commonly used method of pedaling more quickly to a new method of pedaling more slowly. Both groups will work against the maximal force possible. It is expected that the group pedaling more slowly will work against greater force and thus will have improved outcomes compared to other group pedaling faster. Methods: Twenty people with SCI, ages 18-65 years, will be randomly assigned to a treatment group and will participate in three 60-minute sessions per week for 6 months at an outpatient rehabilitation center. All subjects must have complete paralysis of both legs, but may have sensation preserved. Before and after 6 months of exercise, subjects will have an MRI scan to assess muscle size and bone, a dexascan to assess bone, a strength test using electrical stimulation to assess muscle force, an analysis of fat free body tissue, and lab work to measure cholesterol, bone factors that provide insight into bone change, and nutritional status. Relevance: If the protocol of pedaling more slowly results in greater improvements, this technique can be applied to clinical practice. Some people with SCI have FES cycles in their homes and many have been cycling for many years. This new technique may allow them to obtain more benefits than what they currently are receiving from FES cycling. In addition, it is important to maintain overall bone, muscle and cardiovascular health so that people with SCI are health and ready when spinal cord regeneration becomes clinically available.

6. Conditions and Keywords

Primary Disease or Condition Being Studied in the Trial, or the Focus of the Study
Spinal Cord Injury
Keywords
Spinal Cord Injury, Cycling, Functional Electrical Stimulation

7. Study Design

Primary Purpose
Treatment
Study Phase
Phase 2, Phase 3
Interventional Study Model
Parallel Assignment
Masking
None (Open Label)
Allocation
Randomized
Enrollment
17 (Actual)

8. Arms, Groups, and Interventions

Arm Title
High cadence, low resistance
Arm Type
Experimental
Arm Description
Subjects in this arm will cycle with functional electrical stimulation at a higher cadence (speed) and a lower resistance.
Arm Title
Low cadence, high resistance
Arm Type
Experimental
Arm Description
Subjects in this arm will cycle with functional electrical stimulation at a lower cadence (speed) and a higher resistance.
Intervention Type
Other
Intervention Name(s)
Cycling with functional electrical stimulation
Intervention Description
Subjects will cycle with functional electrical stimulation for one hour, 3 times per week at Magee Rehab's outpatient center. Subjects will cycle for a total of 26 weeks (6 months).
Primary Outcome Measure Information:
Title
Bone density and bone microarchitecture
Description
Bone is measured using dexascan and Magnetic Resonance Imaging (MRI) to examine different types of bone (cortical and trabecular).
Time Frame
Baseline
Title
Bone density and bone microarchitecture
Description
Bone is measured using dexascan and Magnetic Resonance Imaging (MRI) to examine different types of bone (cortical and trabecular).
Time Frame
6 months
Title
Muscle volume
Description
Muscle volume is assessed using MRI
Time Frame
Baseline
Title
Muscle volume
Description
Muscle volume is assessed using MRI
Time Frame
6 months
Secondary Outcome Measure Information:
Title
Muscle strength
Description
Muscle strength is assessed by stimulating the muscle using a max twitch technique and measuring the isometric force output on a dynamometer.
Time Frame
Baseline
Title
Muscle strength
Description
Muscle strength is assessed by stimulating the muscle using a max twitch technique and measuring the isometric force output on a dynamometer.
Time Frame
3 months
Title
Muscle strength
Description
Muscle strength is assessed by stimulating the muscle using a max twitch technique and measuring the isometric force output on a dynamometer.
Time Frame
6 months
Title
Bone markers
Description
Bone markers are assessed through blood and urine analysis.
Time Frame
baseline
Title
Bone markers
Description
Bone markers are assessed through blood and urine analysis.
Time Frame
3 months
Title
Bone markers
Description
Bone markers are assessed through blood and urine analysis.
Time Frame
6 months
Title
Fat free soft tissue
Description
Fat free mass is assessed using a bioimpedance monitor.
Time Frame
baseline
Title
Fat free soft tissue
Description
Fat free mass is assessed using a bioimpedance monitor.
Time Frame
3 months
Title
Fat free soft tissue
Description
Fat free mass is assessed using a bioimpedance monitor.
Time Frame
6 months

10. Eligibility

Sex
All
Minimum Age & Unit of Time
18 Years
Maximum Age & Unit of Time
65 Years
Accepts Healthy Volunteers
No
Eligibility Criteria
Inclusion Criteria: Cervical or thoracic SCI of greater than 6 months duration American Spinal Injury Association Impairment Scale (AIS) levels A (motor and sensory complete) or B (motor complete) Intact lower motor neurons to the quadriceps, hamstrings, and gluteal muscles Exclusion Criteria: History of renal or bladder stones or renal impairment Presence of conditions that require chronic steroids Symptomatic or known cardiac disease Pulmonary disease limiting exercise tolerance Ventilator dependency Implanted devices that may be adversely affected by the FES system Lower extremity fragility fractures in the previous 3 months Severe spasticity in legs Presence of a Grade 2 or higher pressure ulcer Severely limited range of joint motion Heterotopic ossification of joints in the lower extremities Uncontrolled autonomic dysreflexia Dislocation of one or both hips Pregnancy or plans to become pregnant during the study Post menopausal, if female Current seizure disorder Participation in activities involving electrical stimulation or activity based therapy within the past 3 months Participation in a neuroregenerative intervention within the past 12 months
Overall Study Officials:
First Name & Middle Initial & Last Name & Degree
Therese E Johnston, PT, PhD, MBA
Organizational Affiliation
Thomas Jefferson University
Official's Role
Principal Investigator
Facility Information:
Facility Name
Magee Rehabilitation Hospital
City
Philadelphia
State/Province
Pennsylvania
ZIP/Postal Code
19102
Country
United States
Facility Name
Thomas Jefferson University Hospital
City
Philadelphia
State/Province
Pennsylvania
ZIP/Postal Code
19107
Country
United States
Facility Name
Thomas Jefferson University
City
Philadelphia
State/Province
Pennsylvania
ZIP/Postal Code
19107
Country
United States

12. IPD Sharing Statement

Citations:
PubMed Identifier
26705884
Citation
Johnston TE, Marino RJ, Oleson CV, Schmidt-Read M, Leiby BE, Sendecki J, Singh H, Modlesky CM. Musculoskeletal Effects of 2 Functional Electrical Stimulation Cycling Paradigms Conducted at Different Cadences for People With Spinal Cord Injury: A Pilot Study. Arch Phys Med Rehabil. 2016 Sep;97(9):1413-1422. doi: 10.1016/j.apmr.2015.11.014. Epub 2015 Dec 17.
Results Reference
derived

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The Effects of Two Functional Electrical Stimulation Cycling Paradigms

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